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Pharmacovigilance Services Associate

1-3 years
Not Disclosed
10 Feb. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Services Associate
Location: Chennai
Job No.: aioc-s01566323
Job Type: Full-time

Job Description

Skill Required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance
Designation: Pharmacovigilance Services Associate
Qualifications: Bachelor of Pharmacy / Bachelor of Physiotherapy / BSc. Nursing
Years of Experience: 1 to 3 years

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities. Visit us at www.accenture.com.

Job Overview:

You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life by enabling them to improve outcomes by converging around the patient and connecting scientific expertise with unique insights into the patient experience.

Your responsibilities include the management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts for both Serious and Non-serious cases. You will be responsible for case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.

What Are We Looking For?

  • Ability to work well in a team
  • Agility for quick learning
  • Adaptable and flexible

Roles and Responsibilities:

  • Solve routine problems, largely through precedent and referral to general guidelines.
  • Expected interactions are within your own team and direct supervisor.
  • Detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments.
  • Decisions will impact your own work.
  • Work as an individual contributor as part of a team, with a predetermined, focused scope of work.
  • This role may require you to work in rotational shifts.